Search Thermo Fisher Scientific
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GGCGGGCAGGATGGTGGTGAGCTGC[A/G]GCCGCTGCAGAGTGAAGGCGCTGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606424 MIM: 612945 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CYP2T1P PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CYP2T1P - cytochrome P450 family 2 subfamily T member 1, pseudogene | ||||||
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There are no transcripts associated with this gene. |
EGLN2 - egl-9 family hypoxia inducible factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_053046.3 | 620 | Missense Mutation | CAG,CGG | Q,R 89 | NP_444274.1 | |
NM_080732.3 | 620 | Missense Mutation | CAG,CGG | Q,R 89 | NP_542770.2 |
MIA-RAB4B - MIA-RAB4B readthrough (NMD candidate) | ||||||
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There are no transcripts associated with this gene. |
RAB4B - RAB4B, member RAS oncogene family | ||||||
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There are no transcripts associated with this gene. |
RAB4B-EGLN2 - RAB4B-EGLN2 readthrough (NMD candidate) | ||||||
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There are no transcripts associated with this gene. |